FierceBiotechFierceBioResearcherFierceVaccinesFiercePharma   FierceHealthcare

FierceBiotech and FiercePharma Jobs

Clinical Supply Manager - PDL BioPharma

May 09
Location: Redwood City, CA
Categories: Clinical
Website: http://pdl.com/careers

Position Description

Drive change and define standards, at PDL Biopharma, Inc.


PDL BioPharma, Inc is a biopharmaceutical company focused on the discovery and development of novel antibodies in oncology and select immunologic diseases. Our current product pipeline includes five breakthrough therapies for acute-care environments. Pioneering science and a rich development pipeline define PDL BioPharma. And our success is based on one key factor – our people. At PDL BioPharma, every employee directly contributes to the development and delivery of innovative therapies that help make real a difference in people’s lives. We foster a goal-oriented and entrepreneurial culture where teamwork, commitment, and initiative are valued and rewarded. PDL BioPharma invites you to be part of the future of biotechnology. We are proud to be an equal opportunity employer.



Manager of Clinical Supplies:.


You enjoy working in a team-powered environment, where your solid organizational skills and critical attention to detail are key. This position is responsible for managing clinical supplies for clinical trials of PDL clinical products. This position will select, manage and oversee clinical labeling, packaging and distribution activities conducted at Contract Manufacturing Organizations (CMO). Reporting to the Director of Supply Chain, this position will have close collaboration with Clinical Operations, Project Management, Process Development, Quality Assurance, Quality Control and the rest of the Supply Chain Organization.

Key Responsibilities:

• Manage labeling, packaging and distribution of clinical materials conducted at CMO’s

• Manage clinical inventory and supply logistics

• Develop forecasts for clinical supplies, in collaboration with Clinical Operations and Project Management

• Develop label specifications in collaboration with Clinical Operations and Regulatory department

• Participate in budgeting process and manage project specific budgets

• Establish cost-effective supply agreements, contracts, quotations and proposals

• Manage performance and development of direct reports to ensure achievement of organizational and department goals

• Travel required domestically and internationally

• Works within GCP Compliance standards environment

• Maintains knowledge of GCP

• Maintains positive and productive relationships with all customers – internally and externally

• Uses professional concepts and company policies and procedures to solve a wide range of problems

• Exercises judgment within generally defined practices and policies to determine appropriate action and solutions

• May perform other duties as necessary or assigned

How to Apply

sarah.shields@pdl.com

Application Instructions / Send a Resume